Canonical Allele Identifier: CA1239490423

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742354C= , CM000664.2:g.25742354C=	GRCh38
NC_000002.11:g.25965223C= , CM000664.1:g.25965223C=	GRCh37
NC_000002.10:g.25818727C=	NCBI36
NG_052995.1:g.141163G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3980G=	ENSP00000337250.5:p.Arg1327=
ENST00000435504.9:c.3983G= MANE Select	ENSP00000391447.3:p.Arg1328=
ENST00000336112.8:c.3899G=	ENSP00000337250.4:p.Arg1300=
ENST00000404843.5:c.2432G=	ENSP00000383920.1:p.Arg811=
ENST00000435504.8:c.3983G=	ENSP00000391447.3:p.Arg1328=
NM_018263.4:c.3983G=	NP_060733.4:p.Arg1328=
XM_006712039.2:c.3617G=	XP_006712102.1:p.Arg1206=
XM_006712040.1:c.3203G=	XP_006712103.1:p.Arg1068=
XM_011532950.1:c.3980G=	XP_011531252.1:p.Arg1327=
XM_011532951.1:c.3809G=	XP_011531253.1:p.Arg1270=
NM_018263.5:c.3983G=	NP_060733.4:p.Arg1328=
XM_006712039.3:c.3617G=	XP_006712102.1:p.Arg1206=
XM_006712040.2:c.3203G=	XP_006712103.1:p.Arg1068=
XM_011532950.3:c.3980G=	XP_011531252.1:p.Arg1327=
XM_011532951.2:c.3809G=	XP_011531253.1:p.Arg1270=
XM_017004430.1:c.3203G=	XP_016859919.1:p.Arg1068=
XM_024452974.1:c.4163G=	XP_024308742.1:p.Arg1388=
NM_001369346.1:c.3809G=	NP_001356275.1:p.Arg1270=
NM_001369347.1:c.3203G=	NP_001356276.1:p.Arg1068=
NM_018263.6:c.3983G= MANE Select	NP_060733.4:p.Arg1328=